Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP286720.RALPbV7N2-W-g_J9yFO9aq0cxNFH2j8aWzEfaKLnKHH3Y130_assertion> ?p ?o ?g. }
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- NP286720.RALPbV7N2-W-g_J9yFO9aq0cxNFH2j8aWzEfaKLnKHH3Y130_assertion type Assertion NP286720.RALPbV7N2-W-g_J9yFO9aq0cxNFH2j8aWzEfaKLnKHH3Y130_head.
- NP286720.RALPbV7N2-W-g_J9yFO9aq0cxNFH2j8aWzEfaKLnKHH3Y130_assertion description "[Missense mutations in CBS are the major cause of inherited HCU (homocystinuria).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP286720.RALPbV7N2-W-g_J9yFO9aq0cxNFH2j8aWzEfaKLnKHH3Y130_provenance.
- NP286720.RALPbV7N2-W-g_J9yFO9aq0cxNFH2j8aWzEfaKLnKHH3Y130_assertion evidence source_evidence_literature NP286720.RALPbV7N2-W-g_J9yFO9aq0cxNFH2j8aWzEfaKLnKHH3Y130_provenance.
- NP286720.RALPbV7N2-W-g_J9yFO9aq0cxNFH2j8aWzEfaKLnKHH3Y130_assertion SIO_000772 22985361 NP286720.RALPbV7N2-W-g_J9yFO9aq0cxNFH2j8aWzEfaKLnKHH3Y130_provenance.
- NP286720.RALPbV7N2-W-g_J9yFO9aq0cxNFH2j8aWzEfaKLnKHH3Y130_assertion wasDerivedFrom befree-20150227 NP286720.RALPbV7N2-W-g_J9yFO9aq0cxNFH2j8aWzEfaKLnKHH3Y130_provenance.
- NP286720.RALPbV7N2-W-g_J9yFO9aq0cxNFH2j8aWzEfaKLnKHH3Y130_assertion wasGeneratedBy ECO_0000203 NP286720.RALPbV7N2-W-g_J9yFO9aq0cxNFH2j8aWzEfaKLnKHH3Y130_provenance.